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A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease

✍ Scribed by Lei Wang; Ji-feng Guo; Li-luo Nie; Qian Xu; Xing Zuo; Qi-ying Sun; Xin-xiang Yan; Bei-sha Tang


Book ID
116771843
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
306 KB
Volume
468
Category
Article
ISSN
0304-3940

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## Abstract To investigate the frequency of mutations in the Leucine‐Rich Repeat Kinase 2 gene (__LRRK2__) in a sample of Austrian Parkinson's disease (PD) patients, we sequenced the complete coding region in 16 patients with autosomal dominant PD. Furthermore, we sequenced exons 31, 35, and 41 add